Posterior Fixation

Posterior semi-rigid osteosynthesis system VEOS PEEK-OPTIMA™ Image Contrast

Semi-rigid posterior osteosynthesis system

VEOS PEEK-OPTIMA™ Image Contrast is a top loading posterior fixation system offering the possibility to perform semi-rigid posterior fixation.

VEOS is part the the VEOS-KAPHORN modular platform of implants and instruments, offering a versatile solution to adapt to surgeon's needs: several specific implants and instruments modules are organized around a universal base.

Fully modular, the platform aims to offer a wide range of possibility in terms of technologies, surgical approaches and treament solutions.

Download the technical sheet Get more information

Informations
Features
Product Range
Regulatory Notices

Informations

VEOS is a top loading posterior fixation system offering the possibility to perform semi-rigid posterior fixation with PEEK-OPTIMA™ rods.

VEOS implants are available in a range of shapes and sizes for screws, locking screws, rods and connectors.

Implants material
• PEEK OPTIMA LT1-6BA (norme ASTM F2026).

Instruments material
• Stainless steel (EN 10088-2, EN 10216-5, ASTM A213), titanium (5832-3 or 5832-2), polymers

Indications
VEOS system can be used in skeletally mature individuals (adults) for the posterior fixation of the lumbar spine.

It is indicated for the treatment of the degenerative spine.

VEOS can also be used in revision surgery in case of failure of a previous procedure.

Features

2 screw options: solid and cannulated-fenestrated
Polyaxial, monoaxial and polyaxial reduction screws
Double threaded solid screw
Quadruple and double threaded cannulated screw
PEEK rods: to perform semi-rigid constructs and help reduce the risk of adjacent segment syndrom
Barium sulfate integrated into PEEK to facilitate imaging controls

Product Range

5 Schraubendurchmesser (ø4,5 bis 8,5 mm) für polyaxiale, monoaxiale und Reduktionsschrauben
Vorgeformte PEEK-OPTIMA™-Stäbe, Durchmesser 5,5 mm. Länge: 40 bis 130 mm

Regulatory Notices

VEOS is a posterior osteosynthesis system. It is intended for the reduction of pathologies of the thoraco-lumbo-sacral spine by restoring the disc height as well as the physiological bending of the spine.

Please read the instructions in the instruction for use carefully.

These implants are Class IIb medical devices CE 0459-marked in accordance with current European regulations.

VEOS implants must be used with a specific set of CE-marked Class I non-invasive instruments and CE 0459-marked Class Ir reusable surgical instruments, in accordance with current European regulations.
The use of these instruments is described in the surgical technique.

Manufacturer
DISTIMP: 7, allée du Moulin Berger 69130 Ecully, France

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Posterior semi-rigid osteosynthesis system VEOS PEEK-OPTIMA™ Image Contrast